This document provides guidance on identifying and mitigating risks associated with digital birth registration for implementing government agencies and their partners operating in low- and middle-income countries. It expands on the model of DBR developed by Plan International as part of its Count Every Child initiative and within the context of strengthening civil registration and vital statistics (CRVS) systems more broadly. The tool provides: checklists of likely risk factors, example risk mitigation mechanisms for each, and prompts to develop context-based responses.

This guide is intended to help build analytical capacity to assess the quality of mortality statistics that are currently being collected in order to improve their value in informing health policies and programs. To assist countries in validating and correcting their mortality data, the World Health Organization (WHO), in partnership with the Health Information Systems Knowledge Hub at the University of Queensland (UQ), Brisbane, has developed this mortality statistics assessment guide and toolkit.

This handbook contains instructions for medical examiners and coroners on the registration of deaths and the reporting of fetal deaths. It was prepared by the Department of Health and Human Services, Centers for Disease Control and Prevention, National Center for Health Statistics (NCHS). These instructions pertain to the 2003 revisions of the U.S. Standard Certificate of Death and the U.S. Standard Report of Fetal Death and the 1992 revision of the Model State Vital Statistics Act and Regulations.

The VAI was initially designed to be used by field reporters with minimal schooling and had only 18 symptom questions. It also allowed for the recording of a brief open-ended narrative, the place of death, any treatment by health services, and the type of treatment. The disease classification was based on Lay reporting of health information (WHO 1978) and COD was entered into the international form of the death certificate. Verbal autopsies (VAs) were physician-coded with reference to diagnostic algorithms.

This document highlights the importance of marriage and divorce registrations in Africa and presents the status of marriage and divorce registration, what is currently being done and recommendations for improvement.

Data2X, named for the power women have to multiply progress in their societies, aims to advance gender equality and women’s empowerment through improved data collection and analysis that can provide a solid evidence-base to guide development policy. To provide basic information for a Data2X roadmap, this report maps gender data gaps in developing countries across five domains of women’s empowerment: (1) health, (2) education, (3) economic opportunities, (4) political participation, and (5) human security.

This document provides an overview of: CRVS in the African context, what is being done to improve CRVS systems in Africa, the benefits of CRVS, the major challenges, and the key elements are that constitute Civil Registration.

These basic guidelines are a tool for countries and regions that have not yet introduced correct cause-of-death certification according to the ICD, or established ICD morbidity and mortality coding practices for their data, and therefore cannot compare the health situation of their population to that of other countries. The tool is organised for easy reference and explains in a stepwise way how to go about establishing ICD certification and coding practices in a country or region.

The main objective of the first International Identity Management (Id-M) Conference, organized by representatives from the Government of Korea (Ministry of Government Administration and Home Affairs), the African Development Bank (AfDB), the Asian Development Bank (ADB), and the Inter-American Development Bank (IDB), was to create synergies and disseminate specialized knowledge regarding the conceptual and practical complexities involved in modernizing civil identity and identification systems.